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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name chamber, oxygen, topical, extremity
510(k) Number K981949
Device Name NUMOBAG
Applicant
NUMOTECH, INC.
21800 OXNARD ST., SUITE 840
WARNER CENTER PLAZA
WOODLAND HILLS,  CA  91367
Applicant Contact W. PATRICK NOONAN
Correspondent
NUMOTECH, INC.
21800 OXNARD ST., SUITE 840
WARNER CENTER PLAZA
WOODLAND HILLS,  CA  91367
Correspondent Contact W. PATRICK NOONAN
Regulation Number878.5650
Classification Product Code
KPJ  
Date Received06/03/1998
Decision Date 02/03/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
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